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临床试验/ITMCTR1900002779
ITMCTR1900002779尚未招募未知

A multicenter randomized, double-blind, parallel controlled, trial for integrated traditional Chinese medicine and western short-course chemotherapy in the treatment of multidrug resistance pulmonary tub

onghua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional study

入排标准

年龄范围
18 至 65(—)
性别
All

入选标准

  • 1. Mycobacterium tuberculosis in sputum (rifampicin resistant) was diagnosd positive by Xpert PCR;
  • 2. BD960 Mycobacterium tuberculosis in sputum was positive for Mycobacterium tuberculosis;
  • 3. The drug sensitivity test of BD960 showed that isoniazid and rifampicin were resistant simultaneously;
  • 4. Conform to the established TCM syndrome standard;
  • 5. Aged 18 to 65 years;
  • 6. Accept the drug treatment voluntarily and sign the informed consent.

排除标准

  • 1. ten items of BD drug sensitivity exclude XDR-TB;
  • 2. the continuous course of disease was more than 5 years and the number of retreatment times was more than 2 times in the past;
  • 3. chest CT showed that the diameter of pulmonary cavity was more than 5cm or the number of cavities was more than 5;
  • 4. with the history of massive hemoptysis;
  • 5. body mass index (BMI) was less than 19;
  • 6. tuberculosis but not Pulmonary tuberculosis, such as lymphoid tuberculosis, bone tuberculosis and brain tuberculosis;
  • 7. family history of mental disease; respiratory failure; severe peptic ulcer; malignant tumor; AIDS; autoimmune disease;
  • 8. legally disabled patients;
  • 9. do not take oral medication;
  • 10. pregnant, preparing pregnant or lactating women;
  • 11. those who are allergic to the test drug and its components;
  • 12. QT interval in ECG is greater than 500 ms after correction;
  • 13. patients with abnormal liver function (ALT more than 1.2 times of the upper limit of normal), or positive for HBsAg, HBeAg and HBcAg at the same time;
  • 14. poor control of blood glucose in diabetic patients (fasting blood glucose > 7mmol/L, postprandial blood glucose > 11mmol/L);
  • 15. the researchers determined that the patients could not complete the treatment in the trial period because of the existence risk of other diseases;
  • 16. those who cannot judge the efficacy or incomplete data, which affect the efficacy or safety judgment.

研究者

发起方
onghua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

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